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Date	Panel	Item	Activity
Filter activities 5 actions
17 Dec 2025	Additional findings_Paediatric v0.279	SNTA1	Zornitza Stark Marked gene: SNTA1 as ready
17 Dec 2025	Additional findings_Paediatric v0.279	SNTA1	Zornitza Stark Gene: snta1 has been classified as Red List (Low Evidence).
17 Dec 2025	Additional findings_Paediatric v0.279	SNTA1	Zornitza Stark Classified gene: SNTA1 as Red List (low evidence)
17 Dec 2025	Additional findings_Paediatric v0.279	SNTA1	Zornitza Stark Gene: snta1 has been classified as Red List (Low Evidence).
27 Aug 2020	Additional findings_Paediatric v0.2	SNTA1	Zornitza Stark gene: SNTA1 was added gene: SNTA1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category B gene,Expert Review Amber Mode of inheritance for gene: SNTA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SNTA1 were set to Long QT syndrome